Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4Q193
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 6 |
GO:0016192 | vesicle-mediated transport | 4 | 6 |
GO:0051179 | localization | 1 | 6 |
GO:0051234 | establishment of localization | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 386 | 390 | PF00656 | 0.577 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.637 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.402 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.553 |
CLV_Separin_Metazoa | 244 | 248 | PF03568 | 0.555 |
DEG_APCC_DBOX_1 | 128 | 136 | PF00400 | 0.425 |
DEG_SPOP_SBC_1 | 2 | 6 | PF00917 | 0.554 |
DEG_SPOP_SBC_1 | 458 | 462 | PF00917 | 0.529 |
DOC_ANK_TNKS_1 | 435 | 442 | PF00023 | 0.542 |
DOC_CKS1_1 | 152 | 157 | PF01111 | 0.682 |
DOC_CYCLIN_RxL_1 | 369 | 376 | PF00134 | 0.476 |
DOC_CYCLIN_yCln2_LP_2 | 409 | 415 | PF00134 | 0.557 |
DOC_MAPK_FxFP_2 | 222 | 225 | PF00069 | 0.483 |
DOC_MAPK_FxFP_2 | 37 | 40 | PF00069 | 0.369 |
DOC_MAPK_gen_1 | 76 | 84 | PF00069 | 0.308 |
DOC_MAPK_MEF2A_6 | 232 | 239 | PF00069 | 0.562 |
DOC_PP1_RVXF_1 | 245 | 252 | PF00149 | 0.492 |
DOC_PP2B_LxvP_1 | 130 | 133 | PF13499 | 0.517 |
DOC_PP2B_LxvP_1 | 307 | 310 | PF13499 | 0.494 |
DOC_PP2B_LxvP_1 | 409 | 412 | PF13499 | 0.564 |
DOC_PP2B_LxvP_1 | 455 | 458 | PF13499 | 0.563 |
DOC_PP2B_LxvP_1 | 512 | 515 | PF13499 | 0.576 |
DOC_PP4_FxxP_1 | 222 | 225 | PF00568 | 0.615 |
DOC_PP4_FxxP_1 | 279 | 282 | PF00568 | 0.545 |
DOC_PP4_FxxP_1 | 37 | 40 | PF00568 | 0.369 |
DOC_PP4_FxxP_1 | 481 | 484 | PF00568 | 0.376 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.378 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.304 |
DOC_USP7_UBL2_3 | 406 | 410 | PF12436 | 0.602 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 430 | 435 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.310 |
LIG_14-3-3_CanoR_1 | 129 | 133 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 177 | 182 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 227 | 235 | PF00244 | 0.579 |
LIG_14-3-3_CanoR_1 | 365 | 375 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 471 | 476 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 76 | 85 | PF00244 | 0.338 |
LIG_Actin_WH2_2 | 113 | 131 | PF00022 | 0.368 |
LIG_APCC_ABBA_1 | 341 | 346 | PF00400 | 0.503 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.517 |
LIG_deltaCOP1_diTrp_1 | 467 | 476 | PF00928 | 0.486 |
LIG_eIF4E_1 | 505 | 511 | PF01652 | 0.500 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.355 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.598 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.511 |
LIG_FHA_1 | 461 | 467 | PF00498 | 0.524 |
LIG_FHA_2 | 129 | 135 | PF00498 | 0.480 |
LIG_FHA_2 | 3 | 9 | PF00498 | 0.599 |
LIG_FHA_2 | 426 | 432 | PF00498 | 0.510 |
LIG_GBD_Chelix_1 | 297 | 305 | PF00786 | 0.538 |
LIG_LIR_Apic_2 | 219 | 225 | PF02991 | 0.607 |
LIG_LIR_Gen_1 | 444 | 450 | PF02991 | 0.354 |
LIG_LIR_Gen_1 | 470 | 479 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 300 | 306 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 433 | 438 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 444 | 448 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 470 | 475 | PF02991 | 0.485 |
LIG_NRBOX | 116 | 122 | PF00104 | 0.304 |
LIG_Pex14_2 | 224 | 228 | PF04695 | 0.496 |
LIG_REV1ctd_RIR_1 | 172 | 181 | PF16727 | 0.406 |
LIG_SH2_CRK | 19 | 23 | PF00017 | 0.369 |
LIG_SH2_CRK | 308 | 312 | PF00017 | 0.512 |
LIG_SH2_NCK_1 | 308 | 312 | PF00017 | 0.483 |
LIG_SH2_SRC | 308 | 311 | PF00017 | 0.480 |
LIG_SH2_STAT3 | 505 | 508 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 304 | 307 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.183 |
LIG_SH2_STAT5 | 445 | 448 | PF00017 | 0.563 |
LIG_SH2_STAT5 | 478 | 481 | PF00017 | 0.385 |
LIG_SH3_3 | 149 | 155 | PF00018 | 0.634 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.285 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.536 |
LIG_SUMO_SIM_par_1 | 336 | 342 | PF11976 | 0.419 |
LIG_TYR_ITIM | 301 | 306 | PF00017 | 0.544 |
LIG_TYR_ITIM | 443 | 448 | PF00017 | 0.361 |
LIG_WRC_WIRS_1 | 171 | 176 | PF05994 | 0.398 |
MOD_CDK_SPxK_1 | 430 | 436 | PF00069 | 0.555 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.506 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.631 |
MOD_CK1_1 | 162 | 168 | PF00069 | 0.508 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.358 |
MOD_CK1_1 | 459 | 465 | PF00069 | 0.485 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.652 |
MOD_CK2_1 | 356 | 362 | PF00069 | 0.524 |
MOD_CK2_1 | 425 | 431 | PF00069 | 0.502 |
MOD_CK2_1 | 461 | 467 | PF00069 | 0.541 |
MOD_CK2_1 | 83 | 89 | PF00069 | 0.441 |
MOD_CMANNOS | 469 | 472 | PF00535 | 0.436 |
MOD_Cter_Amidation | 137 | 140 | PF01082 | 0.632 |
MOD_DYRK1A_RPxSP_1 | 354 | 358 | PF00069 | 0.553 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.629 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.787 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.654 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.497 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.407 |
MOD_GlcNHglycan | 416 | 419 | PF01048 | 0.557 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.304 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.641 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.430 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.571 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.376 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.304 |
MOD_LATS_1 | 363 | 369 | PF00433 | 0.492 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.623 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.183 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.453 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.571 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.598 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.509 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.503 |
MOD_NEK2_1 | 449 | 454 | PF00069 | 0.447 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.352 |
MOD_NEK2_2 | 170 | 175 | PF00069 | 0.463 |
MOD_NEK2_2 | 270 | 275 | PF00069 | 0.550 |
MOD_NEK2_2 | 312 | 317 | PF00069 | 0.447 |
MOD_NEK2_2 | 405 | 410 | PF00069 | 0.552 |
MOD_PKA_1 | 71 | 77 | PF00069 | 0.388 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.555 |
MOD_PKA_2 | 270 | 276 | PF00069 | 0.541 |
MOD_PKA_2 | 425 | 431 | PF00069 | 0.502 |
MOD_PKA_2 | 71 | 77 | PF00069 | 0.347 |
MOD_PKA_2 | 78 | 84 | PF00069 | 0.369 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.457 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.464 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.497 |
MOD_Plk_4 | 425 | 431 | PF00069 | 0.502 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.562 |
MOD_Plk_4 | 471 | 477 | PF00069 | 0.361 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.676 |
MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.533 |
MOD_ProDKin_1 | 430 | 436 | PF00069 | 0.663 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.310 |
MOD_SUMO_rev_2 | 384 | 390 | PF00179 | 0.510 |
TRG_DiLeu_BaEn_1 | 506 | 511 | PF01217 | 0.497 |
TRG_DiLeu_BaLyEn_6 | 18 | 23 | PF01217 | 0.285 |
TRG_DiLeu_BaLyEn_6 | 9 | 14 | PF01217 | 0.466 |
TRG_ENDOCYTIC_2 | 19 | 22 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 303 | 306 | PF00928 | 0.523 |
TRG_ENDOCYTIC_2 | 308 | 311 | PF00928 | 0.532 |
TRG_ENDOCYTIC_2 | 404 | 407 | PF00928 | 0.592 |
TRG_ENDOCYTIC_2 | 445 | 448 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 478 | 481 | PF00928 | 0.385 |
TRG_ER_diArg_1 | 423 | 426 | PF00400 | 0.476 |
TRG_Pf-PMV_PEXEL_1 | 501 | 506 | PF00026 | 0.509 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HW11 | Leptomonas seymouri | 44% | 100% |
A0A3Q8IR86 | Leishmania donovani | 92% | 100% |
A4HPJ2 | Leishmania braziliensis | 76% | 100% |
A4ID71 | Leishmania infantum | 92% | 100% |
E9ATA4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |